Abstract

All enterococci produce a complex polysaccharide called the enterococcal polysaccharide antigen (EPA). This polymer is required for normal cell growth and division and for resistance to cephalosporins and plays a critical role in host-pathogen interaction. The EPA contributes to host colonization and is essential for virulence, conferring resistance to phagocytosis during the infection. Recent studies revealed that the "decorations" of the EPA polymer, encoded by genetic loci that are variable between isolates, underpin the biological activity of this surface polysaccharide. In this work, we investigated the structure of the EPA polymer produced by the high-risk enterococcal clonal complex Enterococcus faecalis V583. We analyzed purified EPA from the wild-type strain and a mutant lacking decorations and elucidated the structure of the EPA backbone and decorations. We showed that the rhamnan backbone of EPA is composed of a hexasaccharide repeat unit of C2- and C3-linked rhamnan chains, partially substituted in the C3 position by α-glucose (α-Glc) and in the C2 position by β-N-acetylglucosamine (β-GlcNAc). The so-called "EPA decorations" consist of phosphopolysaccharide chains corresponding to teichoic acids covalently bound to the rhamnan backbone. The elucidation of the complete EPA structure allowed us to propose a biosynthetic pathway, a first essential step toward the design of antimicrobials targeting the synthesis of this virulence factor.IMPORTANCE Enterococci are opportunistic pathogens responsible for hospital- and community-acquired infections. All enterococci produce a surface polysaccharide called EPA (enterococcal polysaccharide antigen) required for biofilm formation, antibiotic resistance, and pathogenesis. Despite the critical role of EPA in cell growth and division and as a major virulence factor, no information is available on its structure. Here, we report the complete structure of the EPA polymer produced by the model strain E. faecalis V583. We describe the structure of the EPA backbone, made of a rhamnan hexasaccharide substituted by Glc and GlcNAc residues, and show that teichoic acids are covalently bound to this rhamnan chain, forming the so-called "EPA decorations" essential for host colonization and pathogenesis. This report represents a key step in efforts to identify the structural properties of EPA that are essential for its biological activity and to identify novel targets to develop preventive and therapeutic approaches against enterococci.

Highlights

  • All enterococci produce a complex polysaccharide called the enterococcal polysaccharide antigen (EPA)

  • We have previously shown that rhamnopolysaccharide Epa of E. faecalis V583 and OG1RF is not detected in mutants deleted for the epaX gene by the cationic dye alcian blue whereas it appears as a blue band in the wild type (WT) [18, 24]

  • The present study established that E. faecalis EPA is a cell wall rhamnan decorated with phosphopolysaccharide chains corresponding to teichoic acids

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Summary

Introduction

All enterococci produce a complex polysaccharide called the enterococcal polysaccharide antigen (EPA). Several components of the E. faecalis cell envelope have been shown to play important roles during host-pathogen interactions (for reviews, see references 5 and 6) These include lipoteichoic teichoic acids (LTAs); the capsular polysaccharide (CPS), which is variable and nonubiquitous; wall teichoic acids (WTAs); and the enterococcal polysaccharide antigen (EPA). EPA from numerous strains contains rhamnose (Rha), N-acetylgalactosamine (GalNAc), Gal, and N-acetylglucosamine (GlcNAc) [16,17,18] This ubiquitous polymer plays a role in multiple processes such as biofilm formation, adhesion to the intestinal mucus and translocation through epithelial cells, resistance to phagocytosis and to antimicrobials, virulence in various infection models, and phage infection [16, 17, 19,20,21,22,23,24,25]. On the basis of the structural data presented, we propose a functional predictive model of the biosynthetic pathway of EPA

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